A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843265



Internal ID22026908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112075066..112075066hg38UCSC Ensembl
chr11:111945790..111945790hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258343
Supporting Variants
Samples
Known GenesC11orf57
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843265
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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